Shangming Wang , Yunan Chen , Guoping Zhang , Yi Zhang , Bin Chen
{"title":"报废光伏组件背板热解特性综合研究:动力学分析、ReaxFF MD模拟和DFT计算","authors":"Shangming Wang , Yunan Chen , Guoping Zhang , Yi Zhang , Bin Chen","doi":"10.1016/j.jaap.2025.107353","DOIUrl":null,"url":null,"abstract":"<div><div>Comprehensive investigation of the pyrolysis of typical Tedlar-PET-Tedlar (TPT) backsheet was conducted under nitrogen, integrating macro-scale thermal analysis with atomistic simulations using reactive force field molecular dynamics (ReaxFF-MD) and density functional theory (DFT). Thermogravimetric experiments reveal that TPT backsheet undergoes single-stage weight-loss process with activation energy increasing initially and then leveling off to an approximately constant value. The iso-conversional method identified pyrolysis kinetic triplet parameters. Furthermore, the reaction mechanism function was reconstructed and optimized based on an adjustment function, which showed improved accuracy in predicting actual pyrolysis behavior compared to traditional solid-state reaction kinetic models. ReaxFF-MD simulations indicate that random scission of polymer chains dominates the pyrolysis process. The decomposition initiates at the C-O bonds adjacent to ester groups in the polyethylene terephthalate (PET) chains, leading to the formation of terephthalic acid (TPA) as major intermediate. Concerted reaction involving six-membered ring transition state with energy barrier of 210.50 kJ/mol was identified as the dominant pathway in the initial pyrolysis of TPT. Subsequently, dehydrofluorination of polyvinyl fluoride (PVF) side groups occurs with energy barrier of 242.90 kJ/mol, producing HF. Synergistic effect between PVF and PET was observed. Fluorinated radicals generated from PVF can react with radicals such as TPA to form fluorinated carbon compounds. Additionally, HF facilitates the cleavage of ester bonds in PET, thus lowering the initial depolymerization barrier to 174.73 kJ/mol. The reaction network constructed, together with the calculated energy barriers and identified rate-determining steps, provides critical insights for the development of energy-efficient and pollution-reducing pyrolysis processes for end-of-life PV backsheet recycling.</div></div>","PeriodicalId":345,"journal":{"name":"Journal of Analytical and Applied Pyrolysis","volume":"193 ","pages":"Article 107353"},"PeriodicalIF":6.2000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comprehensive study on the pyrolysis characteristics of end-of-life photovoltaic module backsheet: Kinetic analysis, ReaxFF MD simulation and DFT calculation\",\"authors\":\"Shangming Wang , Yunan Chen , Guoping Zhang , Yi Zhang , Bin Chen\",\"doi\":\"10.1016/j.jaap.2025.107353\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Comprehensive investigation of the pyrolysis of typical Tedlar-PET-Tedlar (TPT) backsheet was conducted under nitrogen, integrating macro-scale thermal analysis with atomistic simulations using reactive force field molecular dynamics (ReaxFF-MD) and density functional theory (DFT). Thermogravimetric experiments reveal that TPT backsheet undergoes single-stage weight-loss process with activation energy increasing initially and then leveling off to an approximately constant value. The iso-conversional method identified pyrolysis kinetic triplet parameters. Furthermore, the reaction mechanism function was reconstructed and optimized based on an adjustment function, which showed improved accuracy in predicting actual pyrolysis behavior compared to traditional solid-state reaction kinetic models. ReaxFF-MD simulations indicate that random scission of polymer chains dominates the pyrolysis process. The decomposition initiates at the C-O bonds adjacent to ester groups in the polyethylene terephthalate (PET) chains, leading to the formation of terephthalic acid (TPA) as major intermediate. Concerted reaction involving six-membered ring transition state with energy barrier of 210.50 kJ/mol was identified as the dominant pathway in the initial pyrolysis of TPT. Subsequently, dehydrofluorination of polyvinyl fluoride (PVF) side groups occurs with energy barrier of 242.90 kJ/mol, producing HF. Synergistic effect between PVF and PET was observed. Fluorinated radicals generated from PVF can react with radicals such as TPA to form fluorinated carbon compounds. Additionally, HF facilitates the cleavage of ester bonds in PET, thus lowering the initial depolymerization barrier to 174.73 kJ/mol. The reaction network constructed, together with the calculated energy barriers and identified rate-determining steps, provides critical insights for the development of energy-efficient and pollution-reducing pyrolysis processes for end-of-life PV backsheet recycling.</div></div>\",\"PeriodicalId\":345,\"journal\":{\"name\":\"Journal of Analytical and Applied Pyrolysis\",\"volume\":\"193 \",\"pages\":\"Article 107353\"},\"PeriodicalIF\":6.2000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Analytical and Applied Pyrolysis\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0165237025004061\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Analytical and Applied Pyrolysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0165237025004061","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
Comprehensive study on the pyrolysis characteristics of end-of-life photovoltaic module backsheet: Kinetic analysis, ReaxFF MD simulation and DFT calculation
Comprehensive investigation of the pyrolysis of typical Tedlar-PET-Tedlar (TPT) backsheet was conducted under nitrogen, integrating macro-scale thermal analysis with atomistic simulations using reactive force field molecular dynamics (ReaxFF-MD) and density functional theory (DFT). Thermogravimetric experiments reveal that TPT backsheet undergoes single-stage weight-loss process with activation energy increasing initially and then leveling off to an approximately constant value. The iso-conversional method identified pyrolysis kinetic triplet parameters. Furthermore, the reaction mechanism function was reconstructed and optimized based on an adjustment function, which showed improved accuracy in predicting actual pyrolysis behavior compared to traditional solid-state reaction kinetic models. ReaxFF-MD simulations indicate that random scission of polymer chains dominates the pyrolysis process. The decomposition initiates at the C-O bonds adjacent to ester groups in the polyethylene terephthalate (PET) chains, leading to the formation of terephthalic acid (TPA) as major intermediate. Concerted reaction involving six-membered ring transition state with energy barrier of 210.50 kJ/mol was identified as the dominant pathway in the initial pyrolysis of TPT. Subsequently, dehydrofluorination of polyvinyl fluoride (PVF) side groups occurs with energy barrier of 242.90 kJ/mol, producing HF. Synergistic effect between PVF and PET was observed. Fluorinated radicals generated from PVF can react with radicals such as TPA to form fluorinated carbon compounds. Additionally, HF facilitates the cleavage of ester bonds in PET, thus lowering the initial depolymerization barrier to 174.73 kJ/mol. The reaction network constructed, together with the calculated energy barriers and identified rate-determining steps, provides critical insights for the development of energy-efficient and pollution-reducing pyrolysis processes for end-of-life PV backsheet recycling.
期刊介绍:
The Journal of Analytical and Applied Pyrolysis (JAAP) is devoted to the publication of papers dealing with innovative applications of pyrolysis processes, the characterization of products related to pyrolysis reactions, and investigations of reaction mechanism. To be considered by JAAP, a manuscript should present significant progress in these topics. The novelty must be satisfactorily argued in the cover letter. A manuscript with a cover letter to the editor not addressing the novelty is likely to be rejected without review.